A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14108724



Internal ID21286347
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:24084914..24122334hg38UCSC Ensembl
Innerchr3:24126405..24163825hg19UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg3837421
hg1937421
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111049
Supporting Variants
Samplessample387
Known GenesLINC00691, THRB
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14108724
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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